SRX23787619 GSM8118802_r1 SRP492423 PRJNA1081926 SRS20611145 GSM8118802 GSM8118802 ChIP-Seq GENOMIC ChIP Cells were fixed using 1% formaldehyde for 5 min. The crosslinking reaction was quenched with 125mM glycine. Cells were lysed in swelling buffer 5mM PIPES pH8; 85mM KCL; 0,5% IGEPAL + protease inhibitors). Chromatin was sonicated on a Diagenode Bioruptor300 for 30 min (30s ON/ 30s OFF) on the high setting. At least 20 mg of DNA were used for library preparation using the NEBNext Ultra DNA library prep kit. ChIPseq, 150 bp paired-end reads Illumina NovaSeq 6000 SRX23787620 GSM8118803_r1 SRP492423 PRJNA1081926 SRS20611146 GSM8118803 GSM8118803 ChIP-Seq GENOMIC ChIP Cells were fixed using 1% formaldehyde for 5 min. The crosslinking reaction was quenched with 125mM glycine. Cells were lysed in swelling buffer 5mM PIPES pH8; 85mM KCL; 0,5% IGEPAL + protease inhibitors). Chromatin was sonicated on a Diagenode Bioruptor300 for 30 min (30s ON/ 30s OFF) on the high setting. At least 20 mg of DNA were used for library preparation using the NEBNext Ultra DNA library prep kit. ChIPseq, 150 bp paired-end reads Illumina NovaSeq 6000 SRX23787621 GSM8118804_r1 SRP492423 PRJNA1081926 SRS20611147 GSM8118804 GSM8118804 ChIP-Seq GENOMIC ChIP Cells were fixed using 1% formaldehyde for 5 min. The crosslinking reaction was quenched with 125mM glycine. Cells were lysed in swelling buffer 5mM PIPES pH8; 85mM KCL; 0,5% IGEPAL + protease inhibitors). Chromatin was sonicated on a Diagenode Bioruptor300 for 30 min (30s ON/ 30s OFF) on the high setting. At least 20 mg of DNA were used for library preparation using the NEBNext Ultra DNA library prep kit. ChIPseq, 150 bp paired-end reads Illumina NovaSeq 6000 SRX23787622 GSM8118805_r1 SRP492423 PRJNA1081926 SRS20611148 GSM8118805 GSM8118805 ChIP-Seq GENOMIC ChIP Cells were fixed using 1% formaldehyde for 5 min. The crosslinking reaction was quenched with 125mM glycine. Cells were lysed in swelling buffer 5mM PIPES pH8; 85mM KCL; 0,5% IGEPAL + protease inhibitors). Chromatin was sonicated on a Diagenode Bioruptor300 for 30 min (30s ON/ 30s OFF) on the high setting. At least 20 mg of DNA were used for library preparation using the NEBNext Ultra DNA library prep kit. ChIPseq, 150 bp paired-end reads Illumina NovaSeq 6000 SRX23787623 GSM8118806_r1 SRP492423 PRJNA1081926 SRS20611152 GSM8118806 GSM8118806 ChIP-Seq GENOMIC ChIP Cells were fixed using 1% formaldehyde for 5 min. The crosslinking reaction was quenched with 125mM glycine. Cells were lysed in swelling buffer 5mM PIPES pH8; 85mM KCL; 0,5% IGEPAL + protease inhibitors). Chromatin was sonicated on a Diagenode Bioruptor300 for 30 min (30s ON/ 30s OFF) on the high setting. At least 20 mg of DNA were used for library preparation using the NEBNext Ultra DNA library prep kit. ChIPseq, 150 bp paired-end reads Illumina NovaSeq 6000 SRX23787624 GSM8118807_r1 SRP492423 PRJNA1081926 SRS20611150 GSM8118807 GSM8118807 ChIP-Seq GENOMIC ChIP Cells were fixed using 1% formaldehyde for 5 min. The crosslinking reaction was quenched with 125mM glycine. Cells were lysed in swelling buffer 5mM PIPES pH8; 85mM KCL; 0,5% IGEPAL + protease inhibitors). Chromatin was sonicated on a Diagenode Bioruptor300 for 30 min (30s ON/ 30s OFF) on the high setting. At least 20 mg of DNA were used for library preparation using the NEBNext Ultra DNA library prep kit. ChIPseq, 150 bp paired-end reads Illumina NovaSeq 6000